Alkylation of Zwitterionic Thiooxalic Acid Derivatives

The new S-alkyl thiooxal-1-hydrazono-2-amidrazonium halides 2-4 were synthesized by reaction of the corresponding zwitterionic thiooxalic acid derivatives 1 with alkyl halides in methanol. The structures of compounds 4b and 4d were proven by X-ray structural analysis. Both compounds form an interest...

Descripción completa

Detalles Bibliográficos
Autores principales: Martens, Klaus, Scheunemann, Anke, Drexler, Kerstin, Dehne, Heinz, Reinke, Helmut, Michalik, Manfred
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2001
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6236362/
http://dx.doi.org/10.3390/60600540
_version_ 1783371020380405760
author Martens, Klaus
Scheunemann, Anke
Drexler, Kerstin
Dehne, Heinz
Reinke, Helmut
Michalik, Manfred
author_facet Martens, Klaus
Scheunemann, Anke
Drexler, Kerstin
Dehne, Heinz
Reinke, Helmut
Michalik, Manfred
author_sort Martens, Klaus
collection PubMed
description The new S-alkyl thiooxal-1-hydrazono-2-amidrazonium halides 2-4 were synthesized by reaction of the corresponding zwitterionic thiooxalic acid derivatives 1 with alkyl halides in methanol. The structures of compounds 4b and 4d were proven by X-ray structural analysis. Both compounds form an interesting intermolecular network of hydrogen bonds in the solid state.
format Online
Article
Text
id pubmed-6236362
institution National Center for Biotechnology Information
language English
publishDate 2001
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-62363622018-11-19 Alkylation of Zwitterionic Thiooxalic Acid Derivatives Martens, Klaus Scheunemann, Anke Drexler, Kerstin Dehne, Heinz Reinke, Helmut Michalik, Manfred Molecules Article The new S-alkyl thiooxal-1-hydrazono-2-amidrazonium halides 2-4 were synthesized by reaction of the corresponding zwitterionic thiooxalic acid derivatives 1 with alkyl halides in methanol. The structures of compounds 4b and 4d were proven by X-ray structural analysis. Both compounds form an interesting intermolecular network of hydrogen bonds in the solid state. MDPI 2001-05-31 /pmc/articles/PMC6236362/ http://dx.doi.org/10.3390/60600540 Text en © 2001 by MDPI (http://www.mdpi.org). Reproduction is permitted for noncommercial purposes
spellingShingle Article
Martens, Klaus
Scheunemann, Anke
Drexler, Kerstin
Dehne, Heinz
Reinke, Helmut
Michalik, Manfred
Alkylation of Zwitterionic Thiooxalic Acid Derivatives
title Alkylation of Zwitterionic Thiooxalic Acid Derivatives
title_full Alkylation of Zwitterionic Thiooxalic Acid Derivatives
title_fullStr Alkylation of Zwitterionic Thiooxalic Acid Derivatives
title_full_unstemmed Alkylation of Zwitterionic Thiooxalic Acid Derivatives
title_short Alkylation of Zwitterionic Thiooxalic Acid Derivatives
title_sort alkylation of zwitterionic thiooxalic acid derivatives
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6236362/
http://dx.doi.org/10.3390/60600540
work_keys_str_mv AT martensklaus alkylationofzwitterionicthiooxalicacidderivatives
AT scheunemannanke alkylationofzwitterionicthiooxalicacidderivatives
AT drexlerkerstin alkylationofzwitterionicthiooxalicacidderivatives
AT dehneheinz alkylationofzwitterionicthiooxalicacidderivatives
AT reinkehelmut alkylationofzwitterionicthiooxalicacidderivatives
AT michalikmanfred alkylationofzwitterionicthiooxalicacidderivatives

Ejemplares similares